Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75261583-75261990 | Common:4; Rare:140; Clinvar (benign):4 | ||||
chr17:75271146-75271419 | Common:3; Rare:51 | ||||
chr17:75393754-75394031 | Common:1; Rare:62 | ||||
chr17:75515427-75515667 | Common:3; Rare:70 | ||||
chr17:75667148-75667396 | Common:4; Rare:83 | ||||
chr17:75784548-75784872 | Common:2; Rare:144 | ||||
chr17:75855241-75855693 | Common:1; Rare:128 | ||||
chr17:75904849-75905007 | Common:2; Rare:57 | ||||
chr17:75979063-75979283 | Rare:62; Clinvar:4 | ||||
chr17:75979337-75979490 | Common:1; Rare:39; Clinvar (benign):1 | ||||
chr17:76072496-76072647 | Rare:43 | ||||
chr17:76103695-76103886 | Common:6; Rare:66 | ||||
chr17:76725752-76726094 | Common:1; Rare:95 | ||||
chr17:76726453-76726882 | Common:5; Rare:161 | ||||
chr17:76737318-76737595 | Common:3; Rare:102 |